U.S. flag

An official website of the United States government

Format
Sort by
Choose Destination

Search results

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNTNAP2
(I672V)
Single nucleotide variant
(missense variant)
Cortical dysplasia-focal epilepsy syndrome
GUncertain significance
CNTNAP2
Single nucleotide variant
(splice acceptor variant)
Cortical dysplasia-focal epilepsy syndrome
GLikely pathogenic
CNTNAP2
(R1095Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
Format
Sort by
Choose Destination